Dent Disease with Mutations in OCRL1-Reference-Cited by-同舟云学术

Dent Disease with Mutations in OCRL1

Published:2005-02 Issue:2 Volume:76 Page:260-267
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hoopes Richard R.,Shrimpton Antony E.,Knohl Stephen J.,Hueber Paul,Hoppe Bernd,Matyus Janos,Simckes Ari,Tasic Velibor,Toenshoff Burkhard,Suchy Sharon F.,Nussbaum Robert L.,Scheinman Steven J.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference24 articles.

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4. The oculocerebrorenal syndrome of Lowe (Lowe syndrome);Charnas,2001

5. Loss of chloride channel ClC-5 impairs endocytosis by defective trafficking of megalin and cubilin in kidney proximal tubules;Christensen;Proc Natl Acad Sci USA,2003

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